To evaluate the perception of viscosity of a vaginal moisturizer in postmenopausal women
A unicentric, blind, non-comparative clinical study to prove the perceived efficacy of the research product. It will be necessary 33 female research participants, aged between 45 and 70 years menopause with complaint of vaginal dryness. The participant will remain in the study for one day, making use of the research product in the Research Center. Participants will be divided into 2 groups so that each group observes the viscosity (flow) of the test product in a different anatomical position (lying down and standing) immediately after application of the product, after 15 and 30 minutes. Participants will respond to a subjective assessment using a standardized questionnaire to capture possible feelings of discomfort during the study. A gynecologist will be available to monitor the participants throughout the study.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
33
sodium lactate and combination of polymers (polycarbophil, carbomer and PVM / MA copolymer)
To evaluate subjectively the perceived viscosity change
Perceived viscosity change of the research product from the point of view of the target public under normal conditions of use through a questionnaire
Time frame: Immediately after application, 15 and 30 minutes after application
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